Canonical Allele Identifier: CA8566376
Community Standard Title: NM_021939.4(FKBP10):c.829C>G (p.Pro277Ala)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819311C>G , CM000679.2:g.41819311C>G GRCh38
NC_000017.10:g.39975563C>G , CM000679.1:g.39975563C>G GRCh37
NC_000017.9:g.37229089C>G NCBI36
NG_015860.1:g.11602C>G , LRG_12:g.11602C>G

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.829C>G MANE Select NP_068758.3:p.Pro277Ala
ENST00000321562.9:c.829C>G MANE Select ENSP00000317232.4:p.Pro277Ala
NM_021939.3:c.829C>G , LRG_12t1:c.829C>G NP_068758.3:p.Pro277Ala
ENST00000321562.8:c.829C>G ENSP00000317232.4:p.Pro277Ala
ENST00000455106.1:c.57C>G
ENST00000487489.1:n.442C>G
ENST00000489591.5:c.*239C>G ENSP00000466352.1:n.*239C>G
ENST00000706683.1:c.727+784C>G ENSP00000516497.1:n.727+784C>G
XM_011525099.1:c.829C>G XP_011523401.1:p.Pro277Ala
XM_011525099.3:c.829C>G XP_011523401.1:p.Pro277Ala
XM_011525100.1:c.556C>G XP_011523402.1:p.Pro186Ala
XM_011525100.2:c.556C>G XP_011523402.1:p.Pro186Ala